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Electron-ion coincidence study of photofragmentation of the CdCl2 molecule

✍ Scribed by J.A. Kettunen; J. Niskanen; M. Huttula; M. Vapa; S. Urpelainen; H. Aksela


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
721 KB
Volume
46
Category
Article
ISSN
1076-5174

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✦ Synopsis


In this work, the photofragmentation subsequent to valence and Cd4d photoionization of cadmium dichloride (CdCl(2)) were studied using He I and synchrotron excitation. The measurements were performed with a photoelectron-photoion coincidence (PEPICO) setup, and the connection between the singly ionized electronic states and cationic fragments was investigated. The valence-ionized states were found to lead to CdCl(2)(+), Cd(+) and CdCl(+). The Cd4d(- 1) states were found to lead only to Cl(+) ions. The observed charge transfer effect between Cd and Cl was concluded to take place due to internal conversion or fluorescence decay to dissociating valence states either directly or through consecutive fragmentation. The fragmentation energetics were investigated with molecular ab initio calculations, and the calculated energies were found to agree with the detected fragment appearances.


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## Abstract We have measured the synchrotron‐induced photofragmentation of isolated 2‐deoxy‐D‐ribose molecules (C~5~H~10~O~4~) at four photon energies, namely, 23.0, 15.7, 14.6, and 13.8 eV. At all photon energies above the moleculeβ€²s ionization threshold we observe the formation of a large variety